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Sertoli Cell-Only Syndrome: Behind the Genetic Scenes

Overview
Journal Biomed Res Int
Publisher Wiley
Date 2016 Mar 1
PMID 26925412
Citations 16
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Abstract

Sertoli cell-only syndrome is defined by the complete absence of germ cells in testicular tissues and always results in male infertility. The aetiology often remains unknown. In this paper, we have investigated possible causes of Sertoli cell-only syndrome with a special focus on genetic causes. Our results show that, for a large part of the patients (>23% in an unselected group), the sex chromosomes are involved. The majority of patients had a Klinefelter syndrome, followed by patients with Yq microdeletions. Array comparative genomic hybridization in a selected group of "idiopathic patients" showed no known infertility related copy number variations.

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References
1.
Simoni M, Bakker E, Krausz C . EAA/EMQN best practice guidelines for molecular diagnosis of y-chromosomal microdeletions. State of the art 2004. Int J Androl. 2004; 27(4):240-9. DOI: 10.1111/j.1365-2605.2004.00495.x. View

2.
Levin H . Testicular biopsy in the study of male infertility: its current usefulness, histologic techniques, and prospects for the future. Hum Pathol. 1979; 10(5):569-84. DOI: 10.1016/s0046-8177(79)80100-8. View

3.
Van Assche E, Bonduelle M, Tournaye H, Joris H, Verheyen G, Devroey P . Cytogenetics of infertile men. Hum Reprod. 1996; 11 Suppl 4:1-24; discussion 25-6. DOI: 10.1093/humrep/11.suppl_4.1. View

4.
Menten B, Pattyn F, De Preter K, Robbrecht P, Michels E, Buysse K . arrayCGHbase: an analysis platform for comparative genomic hybridization microarrays. BMC Bioinformatics. 2005; 6:124. PMC: 1173083. DOI: 10.1186/1471-2105-6-124. View

5.
Megraw M, Sethupathy P, Corda B, Hatzigeorgiou A . miRGen: a database for the study of animal microRNA genomic organization and function. Nucleic Acids Res. 2006; 35(Database issue):D149-55. PMC: 1669779. DOI: 10.1093/nar/gkl904. View